• Daiichi Sankyo, Inc. (Bernards, NJ)
    …addressed and managed appropriately. Ability to exercise influence at the senior leadership and/ or executive level wherever GLP/non-GLP/ research programs impacting ... compliance relevant matters and lead any remediation efforts. ResponsibilitiesLeads nonclinical QA function to implement a quality system in...the QA review and approval of GLP and GCLP study protocols, clinical study reports, ICFs, external… more
    HireLifeScience (10/23/24)
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  • Senior Toxicologist, In-vivo Study

    ICF (Reston, VA)
    …Experience as study director and/or study monitor for nonclinical or hazard identification studies . + Familiarity with data tracking system outputs ... growth and expanding client base, we are seeking a ** Senior Toxicologist** to work in our Health Science Portfolio....NIEHS) in conducting and reporting the results of hazard studies and supporting risk assessments of environmental pollutants and… more
    ICF (09/11/24)
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  • Vice President, Quality

    Vera Therapeutics (Brisbane, CA)
    Nonclinical Development to ensure the clinical supply manufacturing activities, nonclinical /clinical study activities are conducted in GxP compliance ... patients suffering from immunological diseases. Position Summary: Reporting into the Senior Vice President, Regulatory and Quality, the Vice President, Quality will… more
    Vera Therapeutics (10/30/24)
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  • Clinical Scientist -First Shift

    Randstad US (Philadelphia, PA)
    …will include supporting data management and data cleaning activities of hematology/oncology studies , supporting the medical monitor in routine trial activities ... in hematology/oncology drug development. You will be responsible for supporting senior Clinical Development staff in formulating and executing the Global Development… more
    Randstad US (11/01/24)
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  • Executive Director, Research QA

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …addressed and managed appropriately. Ability to exercise influence at the senior leadership and/ or executive level wherever GLP/non-GLP/ research programs impacting ... matters and lead any remediation efforts. **Responsibilities** + Leads nonclinical QA function to implement a quality system in...the QA review and approval of GLP and GCLP study protocols, clinical study reports, ICFs, external… more
    Daiichi Sankyo Inc. (11/01/24)
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